A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5397n100



Internal ID20157013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133997524..134267621hg38UCSC Ensembl
chr4:134918679..135188776hg19UCSC Ensembl
chr4:135138129..135408226hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38270098
hg19270098
hg18270098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016559, nsv1020818, nsv1016487, nsv1021393, nsv1028039, nsv1034385, nsv1024165
Samples
Known GenesPABPC4L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5397n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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